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49808-20-0

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49808-20-0 Usage

Uses

6-Mercaptopurine Disulfide is an impurity of 6-Mercaptopurine (M225450, monohydrate) which is an immunosuppressive drug used to treat leukemia. It is also used for pediatric non-Hodgkin’s lymphoma, polycythemia vera, and psoriatic arthritis.

Check Digit Verification of cas no

The CAS Registry Mumber 49808-20-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,9,8,0 and 8 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 49808-20:
(7*4)+(6*9)+(5*8)+(4*0)+(3*8)+(2*2)+(1*0)=150
150 % 10 = 0
So 49808-20-0 is a valid CAS Registry Number.

49808-20-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-(7H-purin-6-yldisulfanyl)-7H-purine

1.2 Other means of identification

Product number -
Other names 6,6-Dipurinylsulfid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:49808-20-0 SDS

49808-20-0Downstream Products

49808-20-0Relevant articles and documents

PEGylated mesoporous silica as a redox-responsive drug delivery system for loading thiol-containing drugs

Zhao, Qinfu,Wang, Chen,Liu, Ying,Wang, Jiahong,Gao, Yikun,Zhang, Xiaojing,Jiang, Tongying,Wang, Siling

, p. 613 - 622 (2014)

In this paper, we describe the development of a redox-responsive delivery system based on 6-mercaptopurine (6-MP)-conjugated colloidal mesoporous silica (CMS) via disulfide bonds. mPEG was modified on the surface of silica to improve the dispersibility and biocompatiblity of CMS by reducing hemolysis and protein adsorption. The CMS carriers with different amounts of thiol groups were prepared to evaluate the impact of modified thiol on the drug loading efficiency. In vitro release studies demonstrated that the CMS nanoparticles exhibited highly redox-responsive drug release. The cumulative release of 6-MP was less than 3% in absence of GSH, and reached more than 70% within 2 h in the presence of 3 mM GSH. In addition, by comparing the cumulative release profiles of CMS-SS-MP@mPEG with their counterparts without the grafting of hydrophilic PEG, it was found that mPEG chains did not hinder the drug release due to the cleavable disulfide bonds and the improved dispersibility. Overall, this work provides a new strategy to connect thiol-containing/thiolated drugs and hydrophilic polymers to the interior and exterior of silica via disulfide bonds to obtain redox-responsive release and improve the dispersibility and biocompatibility of silica.

SELENOTRISULPHIDES FROM MERCAPTOPURINES

Czauderna, Marian,Samochocka, Krystyna

, p. 765 - 768 (2007/10/02)

Products from the reaction of selenium dioxide with 2-mercapto-(2-MP) and 6-mercapto-purines (6-MP) were studied.The molar ratio of selenium dioxide to mercaptopurines was evaluated from u.v. absorption spectra obtained according to a modification of the method of continuous variations.From the results of the stochiometric calculations the products were shown to be seleno-trisulphides and -disulphides.From electrophoretic data equilibrium constans were computed for both reactions.In the presence of an excess of 6-(MP) the derived selenotrisulphide was stable in alkaline solution.

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